13006-59-2 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
1H-Indole-2-carbonitrile,3-methylis used as a building block or intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new drugs and pesticides with improved efficacy and selectivity.
Used in Dye and Pigment Production:
1H-Indole-2-carbonitrile,3-methylserves as a precursor for the production of dyes and pigments. Its aromatic structure and functional groups enable the creation of a variety of colored compounds with different shades and properties, which can be used in various applications such as textiles, plastics, and printing inks.
Used in Materials Science:
1H-Indole-2-carbonitrile,3-methylhas been studied for its potential use in the development of new materials. Its versatile properties, such as its ability to form complexes and its reactivity, make it a promising candidate for the synthesis of advanced materials with unique properties and applications.
Used in Biological Research:
1H-Indole-2-carbonitrile,3-methylhas been investigated for its potential biological activities, including anticancer and anti-inflammatory properties. Its ability to interact with biological targets and modulate cellular processes makes it a valuable compound for the development of new therapeutic agents and the study of biological mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 13006-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13006-59:
(7*1)+(6*3)+(5*0)+(4*0)+(3*6)+(2*5)+(1*9)=62
62 % 10 = 2
So 13006-59-2 is a valid CAS Registry Number.
13006-59-2Relevant academic research and scientific papers
A convenient synthesis of 2-cyano-3-substituted indoles
Denison, Sophie,Hilton, Stephen T.
, p. 2806 - 2808 (2007/10/03)
A new and mild method for the synthesis of 2-cyano-3-substituted indoles is described which is effective on N-unsubstituted indoles.
Intermolecular reactions of indol-2-yl radicals: A new route to 2-substituted indoles
Fiumana, Andrea,Jones, Keith
, p. 1761 - 1762 (2007/10/03)
The generation of indol-2yl radicals and their addition to a variety of radical accepters to prepare 2-substituted indoles is presented.
BENZENESULPHONYLCARBONITRILE OXIDE. VI. PREPARATION AND REACTIONS OF HETEROCYCLIC SULPHONYL OXIMES
Wade, Peter A.,Pillay, Krishna M.
, p. 239 - 242 (2007/10/02)
Pyrrole and indole derivatives react with benzenesulphonylcarbonitrile oxide, 1 (BSNO) generated in situ to give sulphonyl oximes without isolable isoxazoline intermediates.Furan reacts with BSNO to give isoxazoline 5b; treatment with acid affords the corresponding oxime 2b.Reduction of the sulphonyl oximes with aqueous titanium(III) chloride gives nitriles.The sulphonyl oxime 7 derived from indole reacts with tri-n-propylamine and stilbene to give isoxazoline 10.
Cyanation using the Combined Reagent, Triphenylphosphine-Thiocyanogen (TPPT): A New General Route to Indole and Pyrrole Carbonitriles
Tamura, Yasumitsu,Adachi, Masahiro,Kawasaki, Tomomi,Yasuda, Hitoshi,Kita, Yasuyuki
, p. 1132 - 1135 (2007/10/02)
Various types of indoles, pyrroles, and enamines react with the combined reagent, Ph3P-(SCN)2 (TPPT) under mild conditions to give the corresponding cyanated compounds in high yields.The reaction mechanism of the cyanation is discussed.
